Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
  • A61K8/73—Polysaccharides
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
  • A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
  • A61K31/737—Sulfated polysaccharides, e.g. chondroitin sulfate, dermatan sulfate
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
  • A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
  • A61K8/9706—Algae
  • A61K8/9717—Rhodophycota or Rhodophyta [red algae], e.g. Porphyra
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q5/00—Preparations for care of the hair
  • A61Q5/006—Antidandruff preparations
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q5/00—Preparations for care of the hair
  • A61Q5/02—Preparations for cleaning the hair

Definitions

• the present invention relates to the use of particular sulfated polysaccharides as an anti-dandruff agent, particularly in the cosmetic treatment of skin conditions related to the excessive proliferation of Malassezia yeasts on the scalp.
• the invention also relates to a cosmetic treatment method for eliminating and / or reducing dandruff, in particular that caused by yeasts of the genus Malassezia, employing said sulphated polysaccharides.
• the appearance of dandruff corresponding to an desquamative disorder of the scalp, is embarrassing both from the aesthetic point of view and the inconvenience it causes (itching, redness, etc.), so that many people confronted with this problem at varying degrees wish to get rid of it effectively and definitively.
• Dandruff is an excessive and visible desquamation of the scalp resulting from the rapid multiplication of epidermal cells.
• This phenomenon can be provoked in particular by microtrauma of a physical or chemical nature, such as overly aggressive hair treatments, extreme weather conditions, nervousness, diet, fatigue, pollution; but it has been shown that skin conditions are most often the result of a disorder of the microflora of the scalp, and more particularly of the excessive colonization of a yeast belonging to the family of yeasts of the genus Malassezia (formerly called Pytirosporum ovale) and which is naturally present on the scalp.
• topically applied anti-fungal agents To combat dandruff, it is known to use topically applied anti-fungal agents. These agents aim, by their anti-fungal power, to eliminate or control the growth of a resident yeast of the scalp, belonging to the genus Malassezia and its variants (M. ovalis, M. orbiculare, M. furfur, M. globosa. ..).
• anti-dandruff agents are not totally satisfactory in terms of effectiveness (immediate effectiveness or duration of the effect) and / or in terms of impact on the environment.
• the present invention aims to provide non-irritating anti-dandruff agents for the skin and scalp, as effective as known anti-dandruff agents, while having a more favorable impact in terms of the environment (low bioaccumulation and good biodegradability in particular).
• the invention also aims to propose active agents to prevent excessive colonization of the scalp by Malassezia sp, and in particular to limit the desquamative disorder related to the metabolism of Malassezia.
• the Applicant has now found, surprisingly, that the use of certain sulphated polysaccharides as defined below makes it possible to effectively treat the dandruff conditions, in particular those associated with the proliferation of yeast of the genus Malassezia, and to remedy the disadvantages of the prior art. It has been observed that by employing the sulfated polysaccharides defined hereinafter, the number of dandruff and the desquamative disorder generated by Malassezia and their metabolites, such as oleic acid, can be eliminated and / or reduced.
• the present invention therefore relates to the cosmetic use of particular sulfated polysaccharide as defined below as active to prevent and / or treat dandruff of the scalp.
• the subject of the invention is also a cosmetic treatment method for preventing and / or treating dandruff, in particular that caused by yeasts of the genus Malassezia, characterized in that it comprises the application, on the scalp, of minus a sulfated polysaccharide as defined below.
• the use and the method according to the invention are implemented to treat dandruff caused by the proliferation of yeasts of the genus Malassezia on the scalp.
• the sulphated polysaccharides used according to the invention are chosen from dextran sulphate and sulphated polysaccharides derived from the red algae Porphyridium sp.
• the sulfation rate of the polysaccharides can range from 1% to 30% by weight, relative to the weight of the polysaccharide. Preferably this sulfation rate can range from 2% to 25% by weight.
• the polysaccharide may be optionally acetylated.
• the degree of acetylation can range from 0 to 10% by weight (weight ratio of acetyl units relative to the total weight of the polymer).
• the polysaccharide used according to the invention preferably has a weight average molecular weight of between 1000 and 20.10 6 Daltons, preferably between 2000 and 10.10 6 Da, preferably between 5000 and 5.10 6 Da and more preferably between 10,000 and 1 000. .10 6 Da.
• the sulphated polysaccharide used according to the invention may be dextran sulphate.
• the dextran sulphate sold under the trade name "Dextran sulphate sodium knows CG" by the company PK chemicals may be used.
• the sulphated polysaccharide used according to the invention may be chosen from sulphated polysaccharides derived from the red algae Porphyridium sp, such as that sold under the name "Alguard®” by the company Frutarom.
• the application EP-A-31 1496 describes in particular a process for the preparation of such polysaccharides.
• These sulfated polysaccharides contain glucuronic acid, xylose, glucose, sulfated galactose.
• sulfated polysaccharide used according to the invention is advantageously present in a cosmetic composition containing a physiologically acceptable medium.
• Physiologically acceptable medium means a medium compatible with cutaneous tissues such as the skin and the scalp.
• the sulphated polysaccharide used according to the invention may be present in the cosmetic composition in a content ranging from 0.01% to 20% by weight, relative to the total weight of the cosmetic composition, preferably ranging from 0.05% to 15% by weight. weight, preferably ranging from 0.1 to 10% by weight, and more preferably ranging from 0.1 to 5% by weight.
• the physiologically acceptable medium of the composition may more particularly consist of water and optionally of a physiologically acceptable organic solvent chosen, for example, from lower alcohols comprising from 2 to 8 carbon atoms and in particular from 2 to 6 carbon atoms, such as ethanol, isopropanol, propanol, butanol; polyethylene glycols having from 6 to 80 ethylene oxide units and polyols such as propylene glycol, isoprene glycol, butylene glycol, glycerine and sorbitol.
• a physiologically acceptable organic solvent chosen, for example, from lower alcohols comprising from 2 to 8 carbon atoms and in particular from 2 to 6 carbon atoms, such as ethanol, isopropanol, propanol, butanol; polyethylene glycols having from 6 to 80 ethylene oxide units and polyols such as propylene glycol, isoprene glycol, butylene glycol, glycerine and sorbitol.
• compositions according to the invention may be in any of the galenical forms conventionally used for topical application and especially in the form of aqueous, hydroalcoholic solutions, oil-in-water (O / W) or water-in-water emulsions.
• compositions are prepared according to the usual methods.
• the compositions used according to the invention may be more or less fluid and have the appearance of a white or colored cream, an ointment, a milk, a lotion, a serum, a paste, a mousse, shampoo.
• composition used according to the invention comprises adjuvants usually used in the cosmetics field, and especially chosen from water; the oils ; waxes, pigments, fillers, dyes, surfactants, emulsifiers; cosmetic actives, UV filters, polymers, thickeners, film-forming polymers, preservatives, perfumes, bactericides, odor absorbers, antioxidants.
• compositions are those conventionally used in the field under consideration, and for example from 0.01 to 20% of the total weight of the composition.
• This disorder is obtained by the topical application (for 48 hours) of propylene glycol / ethanol / water solution (5/60/35 volume ratio) containing 5% by weight of oleic acid.
• This method is described in the literature to cause the formation of dandruff on the surface of human skin (YM DeAngelis et al., Three Etiologic Facets of Dandruff and Seborrheic Dermatitis: Malassezia Fungi, Sebaceous Lipids, and Individual Sensitivity, J Investigation Dermatol Symp Proc 10: 295-297, 2005).
• the reconstructed skins produced by the company Episkin, are in plates containing a gelled growth medium (GDA3F from Episkin). On reception, the skins were placed in new "deep-well” boxes containing 8.5 ml of GDA3F medium (liquid), then placed in a 37 ° C incubator whose atmosphere is saturated with water and controlled in C0 2 (5%).
• GDA3F gelled growth medium
• the "control" skin received no treatment. On each other skin, 25 ⁇ of solutions were applied.
• the carrier medium is a mixture of propylene glycol / ethanol / water (5/60/35).
• the sulphated polysaccharide is applied at 2% by weight in the carrier medium.
• the polysaccharide tested is dextran sulfate, sold under the commercial reference "Dextran sulfate sodium knows CG" by the company PK Chemicals.
• Example 1b polysaccharide derived from porphyridium
• the polysaccharide obtained from Porphyridium is sold under the name Alguard® by Frutarom.
• Carrageenan 1 sold under the name SATIAGUM UTC 30 by the company Cargill
• Carrageenan 2 sold under the name SATIAGUM UTC 10 by the company Cargill
• the initial solutions of the test products are twice as concentrated as the final test concentration to account for the 1 ⁇ 2 dilution when placed in contact with the Malassezia suspension.
• the test is carried out on the strains Malassezia globosa and Malassezia restricta. Put the Malassezia strains in contact according to the table below:
• the antifungal effect of the sulfated polysaccharide tested was evaluated by the lack of growth of the Malassezia strain tested, relative to the growth control. Inhibitions were noted from 3 to 0 by assessing the density of the culture on the surface of the agar as compared to the growth control of the strain.
• An anti-dandruff shampoo is prepared comprising the following ingredients:
• Cocoyl betaine in aqueous solution Cocoyl betaine in aqueous solution
• An antidandruff lotion is prepared comprising the following ingredients
• the lotion applied to the hair and scalp helps to reduce the appearance of dandruff.

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• Life Sciences & Earth Sciences (AREA)
• Health & Medical Sciences (AREA)
• Animal Behavior & Ethology (AREA)
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• Engineering & Computer Science (AREA)
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• Epidemiology (AREA)
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• Dermatology (AREA)
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• Pharmacology & Pharmacy (AREA)
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• 2011
  • 2011-12-20 FR FR1162109A patent/FR2984126B1/fr active Active
• 2012
  • 2012-12-14 US US14/365,297 patent/US20140315855A1/en not_active Abandoned
  • 2012-12-14 EP EP12815742.7A patent/EP2794012B1/de not_active Not-in-force
  • 2012-12-14 CN CN201280063511.7A patent/CN104039394A/zh active Pending
  • 2012-12-14 ES ES12815742.7T patent/ES2554110T3/es active Active
  • 2012-12-14 WO PCT/FR2012/052936 patent/WO2013093307A1/fr active Application Filing
  • 2012-12-14 JP JP2014548143A patent/JP2015500867A/ja active Pending

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